List of variants in gene CRYM reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001376256.1(CRYM):c.325-12T>C	rs226045	0.27780
NM_001376256.1(CRYM):c.490-12C>T	rs226052	0.09394
NM_001376256.1(CRYM):c.741C>T (p.Tyr247=)	rs34045013	0.01064
NM_001376256.1(CRYM):c.807T>C (p.Phe269=)	rs144588424	0.00398
NM_001376256.1(CRYM):c.761C>T (p.Ala254Val)	rs727505275	0.00006
NM_001376256.1(CRYM):c.343A>G (p.Ile115Val)	rs201490017	0.00004
NM_001376256.1(CRYM):c.907G>A (p.Ala303Thr)	rs727502945	0.00002
NM_001376256.1(CRYM):c.279G>A (p.Gln93=)	rs876657446
NM_001376256.1(CRYM):c.523_524delinsTT (p.Glu175Leu)	rs386789728
NM_001376256.1(CRYM):c.662C>T (p.Ala221Val)	rs876657447
NM_001376256.1(CRYM):c.864C>G (p.Thr288=)	rs14122

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